Special

BtaINT0081093 @ bosTau6

Intron Retention

Gene
ENSBTAG00000001136 | KIAA1324
Description
KIAA1324 [Source:HGNC Symbol;Acc:HGNC:29618]
Coordinates
chr3:34321629-34322216:-
Coord C1 exon
chr3:34322036-34322216
Coord A exon
chr3:34321726-34322035
Coord C2 exon
chr3:34321629-34321725
Length
310 bp
Sequences
Splice sites
5' ss Seq
TCGGTGAGT
5' ss Score
11.11
3' ss Seq
TAGGAGCTCTCATTTGGCAGGCG
3' ss Score
2.74
Exon sequences
Seq C1 exon
GGTAGGAAAATGTCCGTGTGCACTGACAATGTCACCGACCTCCGGATCCCCGAGGGTGAGTCAGGTTTCTCCAAACCCATCACAGCCTACGTGTGCCAGGCGATCATCATTCCCCCAGAGGTGACAGGCTACAAGGCCGGGGTGTCCTCGCAGCCTGTCAGCCTCGCAGACCGGCTTATCG
Seq A exon
GTGAGTACCTCCGTCTTTCTCACCTGTTTGAGTGTGTGTCTGTGTGAAGAGAGAGTGAGTGAGGCTCCCAGACTCTAAGCTAAAAGGCCCCAGGTGAGGGGCCCAACCTCCTGACCTCTGTTTCCGACTCCATCCTGGGGTACCAAGGGCCCCTGGGGCCACTGATAAACCTTTGGTTTGCCCTCTCCTGAGCCACTCAGGGATGTGATGAGATGAAGGAAGGTGGGATGCGAACAGGTATTGGAAGAACTGAAGTGGTTGCCAGCTAAATGCTACTAGTGAGAACTAATTAGGAGCTCTCATTTGGCAG
Seq C2 exon
GCGTGACAACAGATATGACTCTGGATGGCATCACCTCCCCGGCTGAACTTTTCCACCCGGAGTCCCTGGGAATACCGGACGTGATCTTCTTTTATAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSBTAG00000001136:ENSBTAT00000001511:15
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.000 A=NA C2=0.000
Domain overlap (PFAM):

C1:
NO
A:
NA
C2:
NO


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Primers PCR
Suggestions for RT-PCR validation
F:
GGAAAATGTCCGTGTGCACTG
R:
AAAAGAAGATCACGTCCGGTA
Band lengths:
270-580
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]